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Hydrochloric Acid → 5-Methyl-2,3,4,5-tetrahydro-1,4-benzothiazepine

HRID 539955
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HRID 539955 반응식
[CH3:1][C:2]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[S:6][CH2:5][CH2:4][N:3]=1.[BH4-].[Na+].Cl.[OH-].[Na+]>CO.O>[CH3:1][CH:2]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[S:6][CH2:5][CH2:4][NH:3]1
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참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 4311764Sodium borohydrideHCID 200722975-Methyl-2,3-dihydro-1,4-benzothiazepine

생성물 1

HCID 866913675-Methyl-2,3,4,5-tetrahydro-1,4-benzothiazepine수율 93.5%

시약·촉매·용매 2

HCID 887Methanol
용매
HCID 962Water용매

실험 절차

To a solution of 5-methyl-2,3-dihydro-1,4-benzothiazepine (5.92 g, 33.40 mmol) in methanol (100 mL) was added a solution of sodium borohydride (3.16 g, 83.49 mmol) in water (60 mL). After being stirred at room temperature overnight, the reaction mixture was acidified with concentrated hydrochloric acid, and then stirred at room temperature for 30 minutes. After being adjusted to pH 9 with an aqueous solution of sodium hydroxide, the resulting mixture was extracted with ethyl acetate (60 mL×3). The combined organic layers were washed by brine (100 mL), dried over anhydrous sodium sulfate, and concentrated in vacuo to afford 5.6 g of 5-methyl-2,3,4,5-tetrahydro-1,4-benzothiazepine, MS obsd. (ESI+) [(M+H)+] 180.

후처리

  1. stirringstirred at room temperature for 30 minutes
  2. extractionthe resulting mixture was extracted with ethyl acetate (60 mL×3)
  3. washThe combined organic layers were washed by brine (100 mL)
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-3da58bb64faf42fbaaac30334a3f6c04
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08871756B2

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